Add like
Add dislike
Add to saved papers

A liquid metal-based self-adaptive sulfur-gallium composite for long-cycling lithium-sulfur batteries.

Nanoscale 2018 December 14
Lithium-sulfur (Li-S) batteries have been regarded as a promising candidate for energy storage owing to their ultrahigh theoretical capacity and low cost. However, the commercial application of Li-S batteries has been plagued by the huge volume change of sulfur, the insulative nature of solid active materials (S and Li2S) and the polysulfide shuttle. Here, a uniform sulfur-gallium core-shell structure (S@Ga) with an ultrathin liquid gallium shell was prepared by harnessing the reaction between sulfur and gallium via a facile mixing process. In this S@Ga composite, the thin gallium shell not only exhibits the self-adaptive characteristic to perfectly adapt to the varying volume change of sulfur, restraining the polysulfide shuttle, but also acts as a conductive agent to enhance the electronic/ion transmission, improving the rate capacity of the S@Ga cathode. Therefore, the resultant S@Ga cathode exhibits a high capacity of 1295 mA h g-1 at 0.1C and a high cycling stability with a small decay of 0.043% per cycle for 1000 cycles at 1C.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app